NDC 31722-819 – Aripiprazole

Aripiprazole 2 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC31722-819

Product details

Brand name
Aripiprazole
Generic name
Aripiprazole
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205064
Marketed since
April 28, 2015
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Aripiprazole →

Package NDC codes (5)

Package NDCDescriptionSince
31722-819-01100 TABLET in 1 BOTTLE (31722-819-01)Apr 28, 2015
31722-819-05500 TABLET in 1 BOTTLE (31722-819-05)Feb 2, 2024
31722-819-3030 TABLET in 1 BOTTLE (31722-819-30)Apr 28, 2015
31722-819-3110 TABLET in 1 BLISTER PACK (31722-819-31)Apr 28, 2015
31722-819-32250 TABLET in 1 CARTON (31722-819-32)Apr 28, 2015

Recalls mentioning this NDC

Other Aripiprazole products